Paravalvular leak sealing mechanism

ABSTRACT

A collapsible and expandable stent body includes a generally tubular annulus section, one or more prosthetic valve elements mounted to the stent body, and a cuff attached to the stent body. The prosthetic valve is operative to allow flow in an antegrade direction but to substantially block flow in a retrograde direction. The prosthetic heart valve may include paravalvular leak mitigation features in the form of first and second sealing members. The sealing members are attached to the cuff and extend circumferentially around an abluminal surface of the stent body. The sealing members each have an open side facing in a first axial direction and a closed side facing in an opposite second axial direction. Flow of blood in the second axial direction will tend to force blood into the sealing members and cause the sealing members to billow outwardly relative to the stent body, helping to mitigate paravalvular leak.

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation-in-part of U.S. patentapplication Ser. No. 14/501,200, now U.S. Pat. No. 9,668,857, filed Sep.30, 2014, which claims the benefit of the filing date of U.S.Provisional Patent Application No. 61/900,475 filed Nov. 6, 2013, thedisclosures of which are both hereby incorporated by reference herein.

BACKGROUND

The present disclosure relates to heart valve replacement and, inparticular, to collapsible prosthetic heart valves. More particularly,the present disclosure relates to collapsible prosthetic heart valveshaving improved mechanisms to seal against paravalvular leak.

Prosthetic heart valves that are collapsible to a relatively smallcircumferential size can be delivered into a patient less invasivelythan valves that are not collapsible. For example, a collapsible valvemay be delivered into a patient via a tube-like delivery apparatus suchas a catheter, a trocar, a laparoscopic instrument, or the like. Thiscollapsibility can avoid the need for a more invasive procedure such asfull open-chest, open-heart surgery.

Collapsible prosthetic heart valves typically take the form of a valvestructure mounted on a stent. There are two types of stents on which thevalve structures are ordinarily mounted: a self-expanding stent and aballoon-expandable stent. To place such valves into a delivery apparatusand ultimately into a patient, the valve must first be collapsed orcrimped to reduce its circumferential size.

When a collapsed prosthetic valve has reached the desired implant sitein the patient (e.g., at or near the annulus of the patient's heartvalve that is to be replaced by the prosthetic valve), the prostheticvalve can be deployed or released from the delivery apparatus andre-expanded to full operating size. For balloon-expandable valves, thisgenerally involves releasing the valve, assuring its proper location,and then expanding a balloon positioned within the valve stent. Forself-expanding valves, on the other hand, the stent automaticallyexpands as the sheath covering the valve is withdrawn.

Clinical success of a self-expanding valve may be at least partiallydependent on accurate deployment and sealing. For example, inaccuratedeployment and anchoring may result in the leakage of blood between theimplanted heart valve and the native valve annulus, commonly referred toas perivalvular or paravalvular leakage (“PV leak”). In aortic valves,this leakage enables blood to flow from the aorta back into the leftventricle, reducing cardiac efficiency and putting a greater strain onthe heart muscle. Additionally, calcification of the aortic valve mayaffect performance and the interaction between the implanted valve andthe calcified tissue is believed to be relevant to leakage.Additionally, in certain procedures, collapsible valves may be implantedin a native valve annulus without first resecting the native valveleaflets.

BRIEF SUMMARY

One aspect of the present disclosure relates to mechanisms and featuresfor prosthetic valves to facilitate sealing against paravalvular leaks.These mechanisms may include, for example, patches or other types ofmaterial that expand or billow open upon PV leak to create a better sealbetween the prosthetic valve and the native tissue in which theprosthetic valve is implanted.

In one embodiment of the disclosure, a prosthetic heart valve includes astent body including a generally tubular annulus section defining afirst circumferential row of cells. The prosthetic heart valve mayinclude one or more prosthetic valve elements mounted to the stent bodyand operative to allow flow in an antegrade direction but tosubstantially block flow in a retrograde direction through the annulussection. The prosthetic heart valve may further include a cuff attachedto the stent body and positioned on a luminal surface of the stent body.At least one sealing member may be attached to the cuff, the at leastone sealing member having an open side facing in a first axial directionand a closed side facing in a second axial direction opposite to thefirst axial direction so that a flow of blood in the second axialdirection will tend to force blood into the at least one sealing memberand cause the sealing member to billow outwardly relative to the stentbody. The at least one sealing member may have a shape chosen from thegroup consisting of generally triangular, generally trapezoidal, andgenerally semicircular.

In another embodiment of the disclosure, a prosthetic heart valveincludes a stent body including a generally tubular annulus sectiondefining a first circumferential row of cells and a secondcircumferential row of cells distal to the first circumferential row ofcells. The prosthetic heart valve may also include one or moreprosthetic valve elements mounted to the stent body and operative toallow flow in an antegrade direction but to substantially block flow ina retrograde direction through the annulus section. The prosthetic heartvalve my further include a cuff attached to the stent body andpositioned on a luminal surface of the stent body. At least one proximalsealing member may be attached to the cuff and positioned substantiallywithin a cell in the first circumferential row of cells, the proximalsealing member having an open side facing in a first axial direction anda closed side facing in a second axial direction opposite the firstaxial direction so that a flow of blood in the second axial directionwill tend to force blood into the proximal sealing member and cause theproximal sealing member to billow outwardly relative to the stent body.At least one distal sealing member may be attached to the cuff andpositioned substantially within a cell in the second circumferential rowof cells, the distal sealing member having an open side facing in thefirst axial direction and a closed side facing in the second axialdirection so that the flow of blood in the second axial direction willtend to force blood into the distal sealing member and cause the distalsealing member to billow outwardly relative to the stent body.

In yet a further embodiment of the disclosure, a prosthetic heart valveincludes a stent body including a generally tubular annulus section andone or more prosthetic valve elements mounted to the stent body andoperative to allow flow in an antegrade direction but to substantiallyblock flow in a retrograde direction through the annulus section. A cuffmay be attached to the stent body and positioned on a luminal surface ofthe stent body. A sealing member may be attached to the cuff, thesealing member being generally rectangular and having an open sidefacing in a first axial direction and a closed side facing in a secondaxial direction opposite to the first axial direction so that a flow ofblood in the second axial direction will tend to force blood into thesealing member and cause the sealing member to billow outwardly relativeto the stent body. The sealing member may be wrapped around an entirecircumference of the stent body and define a pocket divided into aplurality of regions, each of the regions being in fluid communicationwith adjacent ones of the regions.

In still a further embodiment of the disclosure, a prosthetic heartvalve includes a stent body including a generally tubular annulussection, and one or more prosthetic valve elements mounted to the stentbody and operative to allow flow in an antegrade direction but tosubstantially block flow in a retrograde direction through the annulussection. A cuff may be attached to the stent body and positioned on aluminal surface of the stent body. At least one strut may form a fingerat a proximal end thereof. The finger may be configured to liesubstantially parallel to the stent body when the stent body is in acollapsed condition and may be configured to curve radially outwardlyand distally when the stent body is in an expanded condition, the cuffbeing attached to the finger.

In a further embodiment of the disclosure, a prosthetic heart valveincludes a collapsible and expandable stent body including a generallytubular annulus section and one or more prosthetic valve elementsmounted to the stent body and operative to allow flow in an antegradedirection but to substantially block flow in a retrograde directionthrough the annulus section. A cuff may be attached to the stent body. Afirst sealing member is attached to the cuff, the first sealing memberextending circumferentially around an abluminal surface of the stentbody and having an open side facing in a first axial direction and aclosed side facing in a second axial direction opposite to the firstaxial direction so that a flow of blood in the second axial directionwill tend to force blood into the first sealing member and cause thefirst sealing member to billow outwardly relative to the stent body. Asecond sealing member is attached to the cuff, the second sealing memberextending circumferentially around the abluminal surface of the stentbody and having an open side facing in the first axial direction and aclosed side facing in the second axial direction so that the flow ofblood in the second axial direction will tend to force blood into thesecond sealing member and cause the second sealing member to billowoutwardly relative to the stent body. The first sealing member maydefine a first pocket having a plurality of first regions, each of thefirst regions being in fluid communication with adjacent ones of thefirst regions. Similarly, the second sealing member may define a secondpocket having a plurality of second regions, each of the second regionsbeing in fluid communication with adjacent ones of the second regions.The first sealing member and/or the second sealing member may be wrappedaround an entire circumference of the stent body. The open side of thefirst sealing member and/or the open side of the second sealing membermay be attached to the cuff at spaced locations around a circumferenceof the stent body. The open side of the first sealing member may includea first plurality of openings and the open side of the second sealingmembers may include a second plurality of openings, the first pluralityof openings being offset in a circumferential direction from the secondplurality of openings. The first sealing member may be positioned neareran inflow end of the stent body than the second sealing member. The openside of the first sealing member may be axially spaced apart from theclosed side of the second sealing member. The first sealing member maycomprise an extension of the cuff, the extension being wrapped around aninflow end of the stent body such that the extension is positioned on anabluminal surface of the stent body. A proximal portion of the extensionon the abluminal surface of the stent body may be connected to aproximal portion of the cuff on the luminal surface of the stent bodywith a seam. The first sealing member and/or the second sealing membermay be formed from a separate piece of material from the cuff. The firstsealing member and/or the second sealing member may be formed of asingle piece of material or a plurality of pieces of material. The firstsealing member and/or the second sealing member may be substantiallyrectangular.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a side elevational view of a conventional prosthetic heartvalve.

FIG. 2 is a highly schematic cross-sectional view taken along line A-Aof FIG. 1 and showing the prosthetic heart valve disposed within anative valve annulus.

FIG. 3A is an enlarged partial schematic view of a sealing memberattached to a stent according to an embodiment of the disclosure.

FIG. 3B is a schematic view of an isolated individual sealing member.

FIG. 3C is a schematic view of an isolated series of sealing members.

FIGS. 3D-E are enlarged views showing portions of sealing members havingdifferent fiber orientations.

FIGS. 3F-G are highly schematic longitudinal cross-sections showing asealing member of a valve billowing open to different extents.

FIGS. 3H-I are schematic views of isolated individual sealing memberswith different shapes.

FIG. 4A is an enlarged partial schematic view of a sealing memberattached to a stent according to another embodiment of the disclosure.

FIG. 4B is an enlarged partial schematic view of a sealing memberattached to a stent according to a further embodiment of the disclosure.

FIG. 4C is a schematic view of isolated sealing members arranged in astaggered pattern.

FIG. 5 is an enlarged partial schematic view of a sealing memberattached to a stent according to still another embodiment of thedisclosure.

FIG. 6A is a highly schematic partial longitudinal cross-section of asealing member attached to a stent, with the stent in an expandedconfiguration, according to yet another embodiment of the disclosure.

FIG. 6B is a highly schematic partial longitudinal cross-section of thesealing member and stent of FIG. 6A in a collapsed configuration.

FIG. 7 is an enlarged partial schematic view of two sealing membersattached to a stent according to yet a further embodiment of thedisclosure.

Various embodiments of the present disclosure will now be described withreference to the appended drawings. It is to be appreciated that thesedrawings depict only some embodiments of the heart valve according tothe descriptions herein and are therefore not to be considered limitingof the scope of the present disclosure.

DETAILED DESCRIPTION

As used herein, the term “proximal,” when used in connection with aprosthetic heart valve, refers to the end of the heart valve closest tothe heart when the heart valve is implanted in a patient, whereas theterm “distal,” when used in connection with a prosthetic heart valve,refers to the end of the heart valve farthest from the heart when theheart valve is implanted in a patient. The term “circumferential,” whenused in connection with a prosthetic heart valve, refers to thedirection around the perimeter of the valve. Also, when used herein, thewords “generally” and “substantially” are intended to mean that slightvariations from absolute are included within the scope of the structureor process recited.

FIG. 1 shows a collapsible stent-supported prosthetic heart valve 100known in the art. The prosthetic heart valve 100 is designed to replacethe function of a native tricuspid, bicuspid or unicuspid valve of apatient, such as a native aortic valve. It should be noted that whilethe present disclosure is described predominantly in connection withprosthetic aortic valves and a stent having a shape as illustrated inFIG. 1, the concepts described herein may also be used with prostheticbicuspid valves, such as prosthetic mitral valves, and with stentshaving different shapes, such as those having a flared or conicalannulus section, a less-bulbous aortic section, and the like, and adifferently shaped transition section. Examples of collapsibleprosthetic heart valves are described in International PatentApplication Publication No. WO/2009/042196; U.S. Pat. No. 7,018,406; andU.S. Pat. No. 7,329,278, the disclosures of all of which are herebyincorporated herein by reference.

Prosthetic heart valve 100 will be described in more detail withreference to FIG. 1. Prosthetic heart valve 100 includes expandablestent 102, which may be formed from biocompatible materials that arecapable of self-expansion, such as, for example, shape memory alloyssuch as nitinol. Stent 102 extends from proximal or annulus end 130 todistal or aortic end 132, and includes tubular annulus section 140adjacent the proximal end and aortic section 142 adjacent the distalend. Annulus section 140 has a relatively small cross-section in theexpanded condition, while aortic section 142 has a relatively largecross-section in the expanded condition. Preferably, annulus section 140is in the form of a cylinder having a substantially round cross-sectionand a substantially constant diameter along its length. Transitionsection 141 may taper outwardly from annulus section 140 to aorticsection 142. Each of the sections of stent 102 includes a plurality ofcells 112 connected to one another in one or more annular rows aroundthe stent. For example, as shown in FIG. 1, annulus section 140 may havetwo annular rows of cells 112 and aortic section 142 and transitionsection 141 may each have one or more annular rows of cells. Cells 112in aortic section 142 may be larger than the cells in annulus section140. The larger cells in aortic section 142 better enable prostheticvalve 100 to be positioned in the native valve annulus without the stentstructure interfering with blood flow to the coronary arteries.

Stent 102 may include one or more retaining elements 118 at distal end132 thereof, the retaining elements being sized and shaped to cooperatewith retaining structures provided on the deployment device (not shown).The engagement of retaining elements 118 with retaining structures onthe deployment device helps maintain prosthetic heart valve 100 inassembled relationship with the deployment device, minimizeslongitudinal movement of the prosthetic heart valve relative to thedeployment device during unsheathing or resheathing procedures, andhelps prevent rotation of the prosthetic heart valve relative to thedeployment device as the deployment device is advanced to the targetlocation and the heart valve deployed. In some variations, retainingelements 118 may be disposed near proximal end 130 of heart valve 100.

Prosthetic heart valve 100 includes one or more prosthetic valveelements, such as valve assembly 104, preferably positioned in theannulus section 140 of stent 102 and secured to the stent. Valveassembly 104 includes cuff 106 and a plurality of leaflets 108, whichcollectively function as a one-way valve by coapting with one another,generally allowing blood to flow in an antegrade direction whilesubstantially blocking blood from flowing in a retrograde direction. Asa prosthetic aortic valve, valve 100 has three leaflets 108. However, itwill be appreciated that other prosthetic heart valves with which theactive sealing mechanisms of the present disclosure may be used may havea greater or lesser number of leaflets.

Although cuff 106 is shown in FIG. 1 as being disposed on the luminal orinner surface of annulus section 140, it is contemplated that the cuffmay be disposed on the abluminal or outer surface of the annulus sectionor may cover all or part of either or both of the luminal and abluminalsurfaces. Both cuff 106 and leaflets 108 may be wholly or partly formedof any suitable biological material or polymer such as, for example,polytetrafluoroethylene (PTFE), ultra high molecular weight polyethylene(UHMWPE), polyethylene terephthalate (PET), silicone, urethane, andcombinations of the preceding materials.

Leaflets 108 may be attached along their belly portions to cells 112 ofstent 102, with the commissure between adjacent leaflets attached tocommissure attachment features (“CAFs”) 116. The particular size andshape of CAFs 116 may vary in different valves, for example valves withlarger or smaller diameters may include CAFs that are sized or shapeddifferently than the illustrated CAFs. As can be seen in FIG. 1, eachCAF 116 may lie at the intersection of four cells 112 of stent 102, twoof the cells being adjacent one another in the same annular row, and theother two cells being in different annular rows and lying in end-to-endrelationship. Preferably, CAFs 116 are positioned entirely within theannulus section 140 of stent 102 or at the juncture of annulus section140 and transition section 141. CAFs 116 may include one or more eyeletswhich facilitate the suturing of the leaflet commissure to the stent.

Prosthetic heart valve 100 may be used to replace, for example, a nativeaortic valve, a surgical heart valve, a repair device or a heart valvethat has undergone a surgical procedure. The prosthetic heart valve maybe delivered to the desired site (e.g., near the native aortic annulus)using any suitable delivery device. During delivery, the prostheticheart valve is disposed inside the delivery device in the collapsedcondition. The delivery device may be introduced into a patient using atransfemoral, transapical, transseptal, transaortic, subclavian or anyother percutaneous approach. Once the delivery device has reached thetarget site, the user may deploy prosthetic heart valve 100. Upondeployment, prosthetic heart valve 100 expands so that annulus section140 is in secure engagement within the native aortic annulus. When theprosthetic heart valve is properly positioned inside the heart, it worksas a one-way valve, allowing blood to flow from the left ventricle ofthe heart to the aorta, and preventing blood from flowing in theopposite direction. However, as described in greater detail below, someamount of blood may unintentionally flow in the opposite directionaround the outside of the prosthetic heart valve due to PV leak.

FIG. 2 is a highly schematic cross-sectional illustration of prostheticheart valve 100 disposed within native valve annulus 250. As seen in thefigure, annulus section 140 of stent 102 has a substantially circularcross-section which is disposed within non-circular native valve annulus250. It should be understood that the depiction of native valve annulus250 in FIG. 2, represented as diagonal lines, is not intended torepresent the anatomical shape of the native valve annulus. At certainlocations around the perimeter of heart valve 100, crescent-shaped gaps200 form between the heart valve and native valve annulus 250. Bloodflowing through these gaps and past valve assembly 104 of prostheticheart valve 100 can cause regurgitation and other inefficiencies whichreduce cardiac performance. Such improper fitment may be due to bendingof stent 102 upon application of force, or due to suboptimal nativevalve annulus geometry due, for example, to calcification of nativevalve annulus 250 or to unresected native leaflets. Embodiments ofprosthetic heart valves disclosed herein address PV leak that may occurthrough gaps 200.

FIG. 3A illustrates a portion of prosthetic heart valve 300 according toan embodiment of the disclosure. In particular, prosthetic heart valve300 includes an active sealing mechanism for sealing against PV leak inthe form of one or more sealing members 320. In this example, sealingmembers 320 take the form of parachute-like elements that billow openwhen blood flows in a retrograde direction D_(R) into the parachute-likeelements. If retrograde flow occurs on the abluminal side of valve 300,the blood may enter one or more sealing members 320, causing the sealingmembers to billow open and facilitating the sealing of gap spacesbetween the patient's anatomy and the valve. It should also be noted,for this and other embodiments described herein, sealing members 320 mayhelp seal a gap space between prosthetic valve 300 and the nativeanatomy, even if there is little or no PV leak to cause the sealingmembers to billow open. This may be due to, for example, the additionalmaterial of sealing members 320 filling gap spaces by virtue of thematerial being positioned in those gap spaces.

In the illustrated embodiment, prosthetic heart valve 300 includes anexpandable stent 302 with a plurality of CAFs 316 (only one illustratedin FIG. 3A), which may be similar in many or all respects to stent 102and CAFs 116 of FIG. 1. Stent 302 extends from proximal or annulus end330 to a distal or aortic end (not shown), and includes annulus section340 adjacent the proximal end and an aortic section (not shown) adjacentthe distal end. Each of the sections of stent 302 includes a pluralityof cells 312 connected to one another in one or more annular rows aroundthe stent. For example, as shown in FIG. 3A, annulus section 340 mayhave two annular rows of cells 312, including a first proximalmostcircumferential row of cells 312 a and a second circumferential row ofcells 312 b distal to the first row. Valve 300 may also include cuff306, which may be substantially similar to cuff 106 of FIG. 1.Preferably, cuff 306 has a relatively straight proximal end. In theillustrated embodiment, cuff 306 is positioned on the luminal side ofstent 302 and attached to the stent, for example, by sutures (notillustrated).

Sealing members 320 may take the form of generally triangular patches ofmaterial, although other shapes may be suitable. The triangular patchesmay be attached to cuff 306 during valve assembly, or after valveassembly is otherwise complete. Any suitable attachment method, such assewing, may be used. Preferably, a distal or open side 321 of eachsealing member 320, in this case the distal side of the triangularpatch, is left partially or completely unconnected to cuff 306. Forexample, if sewing the triangular patch to cuff 306, two proximal sides322, 323 of the triangle, meeting at a proximalmost point, are sewn tothe cuff, but the open side 321 of the triangle is not. With thisconfiguration, the open side 321 of sealing member 320 remains capableof opening upon retrograde blood flow, with the open side facing thedistal end of valve 300. Further, the closed proximal sides 322, 323that are connected to cuff 306 restrict blood from exiting through theproximal sides of sealing member 320. Proximal sides 322, 323 may besewn such that open side 321 is loose or floppy, and not taut, therebyenabling blood to flow into sealing member 320. As described above, ifretrograde blood flow does occur on the abluminal side of valve 300, theparachuting or billowing action of sealing members 320 upon bloodflowing into the sealing members facilitates active sealing between theprosthetic heart valve and the native tissue surrounding the valve.

When taking the form of triangular patches, sealing members 320 may beindividual elements, as illustrated in FIG. 3B, or a continuous seriesof elements, as illustrated in FIG. 3C. With sealing members 320 thatare individual elements, a user may individually attach any desirednumber of the sealing members to corresponding portions of valve 300 inany desired pattern or location. Generally, the more sealing members 320that are used, the greater the profile and general bulkiness of valve300. If certain areas of valve 300 are particularly prone to PV leak, itmay be desirable to strategically attach individual sealing members 320to the valve only in those prone areas. For example, an area of valve300 proximal to each CAF 316 may be particularly prone to PV leak.During operation, when valve 300 is closed and the pressure distal tothe valve is greater than the pressure proximal to the valve, aproximally directed force may cause portions of stent 302, such as CAFs316, to pull radially inward, exposing areas of the valve to potentialPV leak. By using individual sealing members 320 only in those areas,sealing against PV leak may be maximized while minimizing the profileand/or bulkiness of valve 300.

Alternatively, sealing members 320 may take the form of a plurality oftriangular patches in series. Although FIG. 3C illustrates three sealingmembers 320 in series, more or less may be acceptable. For example, ifthe first row 312 a of cells 312 includes nine cells spanning thecircumference of annulus section 340, it may be preferable to use ninesealing members 320 connected together as a single element. Thisconfiguration may be particularly convenient, enabling the user tohandle only a single piece of material. In this configuration, sealingmembers 320 may be attached to cuff 306 such that, for each cell 312 ina particular row of cells, one sealing member is positionedsubstantially within each cell. However, this may also be achieved byattaching nine individual sealing members 320 to cuff 306, or by using acombination of individual sealing members and sealing members attachedto one another in series. The term “substantially within” refers to thefact that, although each sealing member 320 is preferably positionedmostly within a particular cell 312 such that it may billow open throughthe cell with relatively little resistance, some minimal amount of thecell structure may overlap a portion of the sealing member.

Each sealing member 320 may be attached to cuff 306, or to both the cuffand stent body 302. Preferably, each sealing member 320 is attached onlyto cuff 306 and is capable of parachuting or billowing open through acell 312 of stent body 302 upon blood entering the sealing member. Byattaching sealing members 320 to cuff 306 only, rather than to both thecuff and stent body 302, the overall bulkiness and/or profile of valve300 may be reduced.

For this and other embodiments described herein, it should also be notedthat sealing members 320, when valve 300 is implanted in a patient, maybe situated sub-annularly, intra-annularly, and/or supra-annularly. Theparticular position of sealing members 320 with respect to the nativeannulus may be affected by, for example, the particular position of thesealing members on stent body 302. There may be particular advantagesand disadvantages of each position. For example, if the sealing membersare positioned supra-annularly, they may be less likely to be distortedby the shape of the native annulus. However, this positioning may bemore likely to result in coronary blockage, a larger profile in arelatively bulky area of the valve, and the positioning may becoincident with the most calcified areas of the native anatomy. If thesealing members are positioned intra-annularly, they may provide forsealing above and below the annulus without causing other physiologicalissues. However, this positioning may lead to interference withanchoring features of a prosthetic valve, which may lead to a higherlikelihood of valve migration or a larger profile in a relatively bulkyarea of the valve. Finally, if the sealing members are positionedsub-annularly, the valve may have a relatively small profile and thesealing members may be coincident with the least calcified portions ofthe native anatomy. However, this positioning may increase thelikelihood of mitral valve or conduction interference, may require alonger delivery device and may result in a decreased tracking ability ofthe valve.

A number of variables may be manipulated to change the way in which, andhow much, each sealing member 320 billows open during retrograde bloodflow. For example, the type of material forming sealing member 320 mayinfluence how it billows open. In particular, forming sealing member 320from a material with high compliance, such as tissue, including bovineor porcine tissue, may cause the sealing member to open to a greaterextent upon retrograde blood flow in comparison to a lower compliancematerial. Similarly, forming sealing member 320 from a thin material maylead the sealing member to open to a greater extent upon retrogradeblood flow in comparison to a thicker material. The method of attachingsealing members 320 to valve 300 may also affect how the sealing membersopen. For example, loosely sewing sealing members 320 to cuff 306, suchthat the sealing members have a relatively large amount of slack, maylead the sealing members to open to a greater extent upon retrogradeblood flow in comparison to a method in which the sealing members haverelatively little slack from being sewn tightly to the cuff.

Still further, features such as orientation of fibers in the materialused to form sealing members 320 may affect performance. For example, ifsealing member 320 is formed from tissue and is attached to valve 300with the fibers of the tissue oriented predominantly circumferentially,the fibers may have a spring-like effect and resist opening. This mayresult in relatively little billowing of sealing member 320 uponretrograde blood flow in comparison to a sealing member attached to thevalve with tissue fibers oriented predominantly longitudinally.Regarding the fiber orientation, FIG. 3D illustrates tissue portionT_(c) in which tissue fibers F_(c) are oriented predominantly in adirection that is substantially circumferential. That is, when sealingmember 320 is attached to valve 300, tissue fibers F_(c) wouldpredominantly align along the circumferential direction of the valve.FIG. 3E illustrates tissue portion T_(L) in which tissue fibers F_(L)are oriented predominantly in a direction that is substantiallylongitudinal, i.e., a direction that, when sealing member 320 isassembled to valve 300, is substantially parallel to the longitudinalaxis of the valve. Sealing members 320 may also be formed so that thepredominant fiber orientation of the tissue is between circumferentialand longitudinal, and may provide for intermediate extents of billowingof the sealing members. Various methods, such as polarized lightmicroscopy, deflection testing and/or tensioning, may be used todetermine the dominant tissue fiber orientation. The above descriptionregarding fiber orientation may also apply to other materials. Forexample, a sealing member made from fabric may also function differentlydepending on the orientation of the fibers in the fabric. However, thedifference in opening of tissue with longitudinal versus circumferentialfiber orientation may be exaggerated in comparison to the difference inopening of fabric with longitudinal versus circumferential fiberorientation.

FIGS. 3F-G illustrate a schematic cross-section of a portion of valve300 with sealing member 320′ (or 320″) attached to cuff 306 and billowedopen through an open portion of stent body 302. In FIG. 3F, sealingmember 320′ may, for example, be thin, with longitudinally orientedfibers, and may be loosely sewn to cuff 306 so that the sealing memberhas a relatively large amount of slack. In FIG. 3G, sealing member 320″may, for example, be thick, with circumferentially oriented fibers, andmay be tightly sewn to cuff 306 so that the sealing member has arelatively small amount of slack. All else being equal, a given amountof retrograde blood flow may cause sealing member 320′ of FIG. 3F tobillow open to a greater extent than sealing member 320″ of FIG. 3G.These variables may be manipulated such that sealing member 320 opens adesired amount upon exposure to retrograde blood flow. In fact, it maybe desirable to pre-shape the sealing members such that they have anopen configuration, but still may be crimped along with the prostheticvalve during delivery such that, upon delivery into a final expandedconfiguration, the sealing member returns to an original open shape thattends to maximize the ability to capture retrograde blood flow therein.

Sealing member 320 may also take shapes other than generally triangular.For example, FIG. 3H shows a sealing member 325 that has a generallysemicircular shape, while FIG. 3I shows a sealing member 326 that has agenerally trapezoidal shape. However, it should be understood thatshapes other than those specifically disclosed herein may be suitablefor use as a sealing member. Considerations that may be relevant to thesuitability of such an alternate shape include the extent to which thealternate shape matches the shape of the cell 312 through which itbillows open. For example, when attaching a sealing member with analternate shape to cuff 306 and inside stent body 302, the shapepreferably allows the sealing member to open through the open portion ofthe particular cell 312. A sealing member with a shape similar to thatof the cell 312 through which it opens may be able to open relativelyeasily upon retrograde blood flow, while the matching shape may maximizethe volume of blood capable of entering the sealing member. Further, asealing member with a straight, curved, or otherwise non-pointedproximal side, such as the curved proximal side of sealing member 325 orthe straight proximal side of sealing member 326, may provide benefitsover sealing members with pointed proximal sides, such as generallytriangular sealing member 320. In particular, a pointed proximal sidemay tend to cause blood trapped therein to stagnate, while a non-pointedproximal side may reduce the tendency for blood to stagnate, therebyreducing the likelihood of the formation of a thrombus, for example.Further, the pointed proximal side of such a sealing member may notprovide an adequate volume into which blood may flow compared to asimilar shape with a non-pointed proximal side.

The width of the open sides of the sealing members, such as open side321 of sealing member 320, may also be varied. For example, the sealingmembers may have wider openings than those illustrated to maximize thelikelihood of capturing retrograde blood flow. The wide openings, or anyother sealing member openings described herein, may also alternately bepunctuated by frequent stitches or other mechanisms to close portions ofthe open side. The effect of frequently spaced sutures, for example, maycreate a number of smaller openings that still allow blood flow to enterthe particular sealing member. However, if a thrombus forms within thesealing member, the reduced sized openings may make it less likely thatthe thrombus may exit the sealing member into the blood flow.

FIG. 4A illustrates a portion of prosthetic heart valve 400 according toanother embodiment of the disclosure. Prosthetic heart valve 400 may besimilar or identical to prosthetic heart valve 300 in all respects otherthan the active sealing mechanism. For example, prosthetic heart valve400 includes an expandable stent 402 with a plurality of CAFs 416 (onlyone illustrated in FIG. 4A). Stent 402 extends from proximal or annulusend 430 to a distal or aortic end (not shown), and includes annulussection 440 adjacent the proximal end and an aortic section (not shown)adjacent the distal end. Each of the sections of stent 402 includes aplurality of cells 412 connected to one another in one or more annularrows around the stent. For example, as shown in FIG. 4A, annulus section440 may have two annular rows of cells 412, including a firstproximalmost row of cells 412 a and a second row of cells 412 b distalto the first row. Valve 400 may also include cuff 406, which may besubstantially similar to cuff 306 of FIG. 3A. In the illustratedembodiment, cuff 406 is positioned on the luminal side of stent 402 andattached to the stent, for example, by sutures (not illustrated).

Prosthetic heart valve 400 includes sealing members 420 that provide anactive sealing mechanism for sealing against PV leak. Similar to valve300, the sealing members 420 take the form of generally triangularpatches or parachute-like members that billow open when blood flows intothem. However, valve 400 includes proximal sealing members 420 apositioned along the first row of cells 412 a as well as distal sealingmembers 420 b positioned along the second row of cells 412 b. All of theconsiderations discussed above with respect to sealing members 320 ofFIG. 3A apply with equal force to sealing members 420 a and 420 b ofFIG. 4A. Sealing members 420 b on the second row of cells 412 b mayprovide for additional sealing against PV leak. For example, points atwhich open sides 421 a of two adjacent sealing members 420 a meet may beless likely to catch retrograde blood flow. In the illustratedembodiment, a second row of sealing members 420 b is positioned suchthat center portions of the open sides 421 b of sealing members 420 bgenerally align longitudinally with points at which open sides 421 a oftwo adjacent sealing members 420 a meet. In other words, the position ofthe center of open sides 421 a of the first row of sealing members 420 ais circumferentially staggered or offset from the position of the centerof open sides 421 b of the second row of sealing members 420 b. Thisconfiguration may decrease the likelihood that retrograde blood flowwill travel proximally between two adjacent sealing members 420 awithout being caught in any sealing member.

As described with respect to sealing members 320, sealing members 420 a,420 b may be individually attached to cuff 406, or multiple sealingmembers may first be connected to one another in a series forconvenience. For example, in one embodiment, sealing members 420 a, 420b may be attached to cuff 406 at each cell 412 in the first and secondrows of cells 412 a, 412 b, respectively. Also as described with respectto sealing members 320, sealing members 420 a, 420 b may be placedstrategically on valve 400 to maximize sealing against PV leak whileminimizing the number of the sealing members, and therefore minimizingthe bulk of the valve. One embodiment that may be particularlyeffective, illustrated in FIG. 4B, includes only a single sealing member420 b on the cells 412 in the second row of cells 412 b that aredirectly proximal to each CAF 416. For each sealing member 420 b on thesecond row of cells 412 b, two sealing members 420 a are positioned onthe first row of cells 412 a below the sealing member 420 b, such thatthe center portion of the open side 421 b of the sealing member 420 bgenerally aligns longitudinally with the point at which the open sides421 a of the adjacent sealing members 420 a meet.

A number of alternate configurations of sealing members may be utilized.As described above, sealing members, such as sealing members 420 a and420 b, may be positioned on the inner diameter of stent body 402, thatis, between the stent body and cuff 406. However, they may alternatelybe placed on the outer diameter of stent body 402. If positioned on theouter diameter, more shapes and configurations may be used since thesealing members no longer need to be capable of billowing open throughthe open cells of stent body 402. Rather, if on the outer diameter ofstent body 402, the positions of open cells of stent body 402 do notlimit the shape or configuration of the sealing members at all. Forexample, FIG. 4C illustrates a schematic view of sealing members 420 a,420 b arranged in a staggered pattern, with the remainder of prostheticvalve 400 not illustrated. In this configuration, a first row of sealingmembers 420 a is positioned in a staggered relationship with a secondrow of sealing members 420 b. Open sides 421 a of sealing members 420 aare positioned proximally relative to open sides 421 b of sealingmembers 420 b. However, there is some overlap between sealing members420 a, 420 b. In particular, open sides 421 a of sealing members 420 aare positioned approximately at a midline of sealing members 420 b. Inother words, the proximal-to-distal distance between open sides 421 band 421 a is approximately equal to the proximal-to-distal distancebetween open sides 421 a of sealing members 420 a and the proximalmostpoints of sealing members 420 b. These distances may be varied, however,to increase or decrease the level of staggering and overlap betweensealing members 420 a and 420 b. It should further be noted that, inthis particular embodiment, it may be preferable for sealing members 420a, 420 b to be attached to the outer diameter of stent body 402, ratherthan between the stent body 402 and cuff 406. This may be preferable ifthe shape and position of sealing members 420 a, 420 b does not matchwith the shape and position of the open cells of stent body 402 suchthat the sealing members may easily billow open through the open cells.By staggering sealing members 420 a, 420 b, the profile of valve 400 maybe reduced in comparison to a configuration in which sealing members 420a, 420 b are aligned in a single non-staggered row. Still further, itshould be noted that in the embodiments described herein, one row, tworows, or more rows of sealing members may be suitable for use with aprosthetic heart valve.

FIG. 5 illustrates a portion of prosthetic heart valve 500 according toa further embodiment of the disclosure. Prosthetic heart valve 500 maybe similar or identical to prosthetic heart valves 300 and 400 in allrespects other than the active sealing mechanism. For example,prosthetic heart valve 500 includes an expandable stent 502 with aplurality of CAFs 516 (only one illustrated in FIG. 5). Stent 502extends from proximal or annulus end 530 to a distal or aortic end (notshown), and includes annulus section 540 adjacent the proximal end andan aortic section (not shown) adjacent the distal end. Each of thesections of stent 502 includes a plurality of cells 512 connected to oneanother in one or more annular rows around the stent. For example, asshown in FIG. 5, annulus section 540 may have two annular rows of cells512, including a first proximalmost row of cells 512 a and a second rowof cells 512 b distal to the first row. Valve 500 may also include acuff 506, which may be substantially similar to cuffs 306 and 406 ofFIGS. 3A and 4A, respectively. In the illustrated embodiment, cuff 506is positioned on the luminal side of stent 502 and attached to thestent, for example, by sutures (not illustrated).

Prosthetic heart valve 500 includes a sealing member 520 that providesan active sealing mechanism for sealing against PV leak. Sealing member520 may take the form a rectangular patch that functions as aparachute-like member that billows open when blood flows into it. In theillustrated embodiment, sealing member 520 includes an open distal side521 and a closed proximal side 522. The proximal side 522 of sealingmember 520 may be attached, for example by sewing, to cuff 506. Theattachment is preferably such that blood entering sealing member 520cannot exit through the closed proximal side 522 of the sealing member.In this configuration, sealing member 520 defines a pocket. The pocketmay include regions defined by the points at which sealing member 520near the open side 521 is attached to cuff 506, as described below. Eachregion of the pocket may be in fluid communication with adjacentregions. The rectangular patch may be wrapped around the entirecircumference of stent 502 with ends of the patch attached to oneanother to secure the patch in a desired position. In this embodiment,sealing member 520 is a separate entity from cuff 506. Further, in thisembodiment, sealing member 520 is preferably attached over the outsideof both cuff 506 and stent 502 to allow the sealing member to billowopen. This is in contrast to other embodiments, such as generallytriangular sealing members 320, which preferably are attached betweencuff 306 and stent 302 and which are capable of billowing open throughcells 312 of the stent.

One or more individual rectangular patches may be individually attachedto stent 502 such that the collective patches are wrapped partially, orentirely, around the circumference of the stent. Portions of sealingmember 520 near the open side 521 are also preferably attached to cuff506, for example using sutures S. As illustrated, a small number ofstitches, such as two or three, connect distal portions of sealingmember 520 to cuff 506 at spaced locations around the circumference ofthe sealing member. While the sutures S are shown as attaching sealingmember 520 to cuff 506 along portions of the struts where adjacent cells512 a meet, the connections may be made at any point on the cuff. Thedistal attachments preferably are few enough to leave a substantialportion of open side 521 free such that retrograde blood flow may freelyflow into sealing member 520, while still providing enough support tomaintain the position of the distal end of the sealing member relativeto cuff 506. Similar to embodiments described above, if blood flows inthe retrograde direction, represented by arrows D_(R), on the abluminalside of the valve 500, the blood may flow into sealing member 520between the points at which the sealing member is attached to cuff 506.The blood may enter and fill sealing member 520, causing it to expandsimilar to an inner tube, facilitating the creation of a seal against PVleak between valve 500 and the native tissue in which the valve ispositioned.

Sealing member 520 may alternately be formed as an extension of cuff506, rather than one or more separate rectangular patches. For example,cuff 506, which is positioned on the luminal side of valve 500, mayinclude a portion which extends beyond the proximal end of stent 502.This extending portion may be folded or wrapped around the proximal endof stent 502 such that the extending portion is on the abluminal side ofvalve 500. The extending portion would form sealing member 520 and wouldotherwise act similarly to separate rectangular patches attached to cuff506. In this embodiment, in which sealing member 520 is an extension ofcuff 506, it may not be necessary to suture or otherwise attach theproximal end of the sealing member to the cuff, since the sealing memberis an extension of the cuff. However, it still may be preferable to forma seam, for example with a suture, between sealing member 520 and cuff506 adjacent the proximal ends thereof. This may, for example, providestructural support to sealing member 520.

FIG. 6A illustrates a sealing member 620 according to another embodimentof the disclosure. FIG. 6A is a highly schematic sectional view of aproximal portion of a stent body 602 for use in a prosthetic heartvalve. As illustrated, a strut of stent body 602 extends proximally fromCAF 616 to a proximal end of the stent, at which point the struttransitions into a finger 650 that curves radially outwardly anddistally in a general “J” shape. In other words, the strut forms finger650 at a proximal end of the strut. Cuff 606 may be attached on theluminal side of stent 602 and extend toward the proximal end of thestent, and then curve back up radially outwardly and distally, followingthe contour of finger 650. In this embodiment, cuff 606 may extendpartially or completely around the circumference of stent 602, attachedto a discrete number of fingers 650. This embodiment functions similarlyto the embodiment described above in which sealing member 520 forms anextension of cuff 506 that is folded or wrapped over the proximal end ofstent 502. However, the use of fingers 650 may be beneficial, as thearms may be set to curve outwardly only after stent 602 is deployed andtransitions from a collapsed condition to an expanded condition. Forexample, FIG. 6B illustrates stent 602 and finger 650, along with cuff606 and sealing member 620, prior to deployment when it is in acollapsed condition, for example within a delivery device. In thisconfiguration, finger 650 lies substantially flat with respect to stentbody 602. This configuration allows for the collapsed profile to remainrelatively small, since finger 650 and sealing member 620 do not curveoutwardly until stent 602 is released from a delivery device andtransitions into the expanded condition illustrated in FIG. 6A. Once inthe expanded condition, retrograde blood flowing into the sealing member620 may cause the sealing member to expand further or fill up like aninner tube, helping to create a seal between the valve and the nativetissue in which the valve is implanted.

FIG. 7 illustrates a portion of prosthetic heart valve 700 according toa further embodiment of the disclosure. Prosthetic heart valve 700 maybe similar or identical to prosthetic heart valve 500 in most respects.For example, prosthetic heart valve 700 includes an expandable stent 702with a plurality of CAFs 716 (only one illustrated in FIG. 7). Stent 702extends from a proximal or annulus end 730 to a distal or aortic end(not shown), and includes annulus section 740 adjacent the proximal endand an aortic section (not shown) adjacent the distal end. It should beunderstood that, when implanted in a native aortic or pulmonary valve,the proximal end may be referred to as the inflow or inlet end, and thedistal end may be referred to as the outflow or outlet end. It shouldfurther be understood that, if placed in a native atrioventricular valvesuch as the mitral valve, a proximal end of the stent may be referred toas an outflow end.

Each of the sections of stent 702 includes a plurality of cells 712connected to one another in one or more annular rows around the stent.For example, as shown in FIG. 7, annulus section 740 may have twoannular rows of cells 712, including a first proximalmost row of cells712 a and a second row of cells 712 b distal to the first row. Valve 700may also include a cuff 706, which may be substantially similar to cuff506 of FIG. 5. In the illustrated embodiment, cuff 706 is positioned onthe luminal side of stent 702 and attached to the stent, for example, bysutures (not illustrated).

Prosthetic heart valve 700 includes sealing members 720 a, 720 b thatprovide an active sealing mechanism for sealing against PV leak. Sealingmembers 720 a and 720 b may each take a similar or identical form assealing member 520 of prosthetic heart valve 500. For example, sealingmember 720 a may be a rectangular patch that functions as aparachute-like member that billows open when blood flows into it. In theillustrated embodiment, sealing member 720 a includes an open distalside 721 a and a closed proximal side 722 a. The proximal side 722 a ofsealing member 720 a may be attached, for example by sewing, to cuff706. The attachment is preferably such that blood entering sealingmember 720 a cannot exit through the closed proximal side 722 a of thesealing member. In this configuration, sealing member 720 a defines apocket. The pocket may include regions defined by the points at whichsealing member 720 a near the open side 721 a is attached to cuff 706,as described below. Each region of the pocket may be in fluidcommunication with adjacent regions. The rectangular patch may bewrapped around the entire circumference of stent 702 with ends of thepatch attached to one another to secure the patch in a desired position.In this embodiment, sealing member 720 a is a separate entity from cuff706. Further, in this embodiment, sealing member 720 a is preferablyattached over the outside of both cuff 706 and stent 702 to allow thesealing member to billow open.

Sealing member 720 a may take the form of a single rectangular patch, ormultiple patches connected to one another to form a rectangular patchthat is long enough to extend around the entire circumference of annulusportion 740. Portions of sealing member 720 a near the open side 721 aare also preferably attached to cuff 706, for example using sutures 51.As illustrated, a small number of stitches, such as two or three,connect distal portions of sealing member 720 a to cuff 706 at spacedlocations around the circumference of the sealing member. In particular,the sutures 51 may be placed near where one cell 712 a meets acircumferentially adjacent cell 712 a, so that the pocket formed insealing member 720 a has a plurality of openings, each of which having awidth substantially equal to a maximum circumferential width of a cell712 a when stent 702 is in the expanded condition. While the sutures 51are shown as attaching sealing member 720 a to cuff 706 along portionsof the struts where adjacent cells 712 a meet, the connections mayalternatively be made at any point on the cuff. The distal attachmentspreferably are few enough to leave a substantial portion of open side721 a free such that retrograde blood flow may freely flow into sealingmember 720 a, while still providing enough support to maintain theposition of the distal end of the sealing member relative to cuff 706.

Valve 700 may include a second sealing member 720 b, which may take theform of a rectangular patch similar or identical to sealing member 720 a(or similar to any described alternative way to form sealing member 720a). Sealing member 720 b may be positioned mostly or entirely distal tosealing member 720 a, so that a closed proximal side 722 b of sealingmember 720 b is positioned adjacent to or spaced apart from the opendistal side 721 a of sealing member 720 a. Closed proximal side 722 bmay be attached to cuff 706 with sutures or any other suitable fasteningmechanism so that blood entering sealing member 720 b from the open side721 b is unable to exit sealing member 720 b through the closed side 722b. Similar to sealing member 720 a, the open side 721 b of sealingmember 720 b may be coupled to cuff 706 and/or struts of stent 702 atcircumferentially spaced apart locations to form a plurality of openingsleading into the pocket of sealing member 720 b. In the illustratedembodiment, sutures S2 attach portions of the distal side of sealingmember 720 b at locations of cuff 706 and/or stent 702 at which a cell712 b in the second circumferential row meets a circumferentiallyadjacent cell 712 b in that same row. With this configuration, theopenings in open side 721 b of sealing member 720 b generally correspondto the maximum width of a cell 712 b in the expanded condition of stent702. This allows for circumferential positional staggering of theopenings in the open side 721 b of sealing member 720 b compared to theopenings in the open side 721 a of sealing member 720 a.

Similar to embodiments described above, if blood flows in the retrogradedirection, represented by arrows D_(R), on the abluminal side of valve700, the blood may flow into sealing member 720 a between the points atwhich the sealing member is attached to cuff 706. The blood may enterand fill sealing member 720, causing it to expand similar to an innertube, facilitating the creation of a seal against PV leak between valve700 and the native tissue in which the valve is positioned. To theextent that retrograde blood flow is less likely to enter sealing member720 a at the positions at which open side 721 a is sutured to the cuff706 and/or stent 702, such retrograde blood flow may be likely to entersealing member 720 b since the corresponding locations of open side 721b of sealing member 720 b will be free to open and receive retrogradeblood flow. In other words, the use of two sealing members 720 a-b withthe attachment locations described above may provide for similaradditional capability of mitigating PV leak as described in connectionwith the circumferentially staggered patches 421 a-b of FIG. 4A.

Similar to sealing member 520, first sealing member 720 a mayalternately be formed as an extension of cuff 706, with cuff 706including a portion which extends beyond the inflow edge of stent 702.This extending portion may be folded or wrapped around the inflow edgeof stent 702 such that the extending portion is on the abluminal side ofvalve 700. The extending portion would form first sealing member 720 andwould otherwise act similarly to a rectangular patch attached to cuff706. In this embodiment, in which first sealing member 720 a is anextension of cuff 706, it may not be necessary to suture or otherwiseattach the proximal end of the first sealing member 720 a to the cuff706, since the sealing member is an extension of the cuff. However, itstill may be preferable to form a seam, for example with a suture,between first sealing member 720 a and cuff 706 adjacent the proximalends thereof. This may, for example, provide structural support to firstsealing member 720 a.

Still further, first sealing member 720 a and/or second sealing member720 b may be configured to wrap around only a part of the circumferenceof stent 702. This may allow, for example, strategic placement ofsealing members 720 a and/or 720 b to maximize the likelihood of thesealing members 720 a and/or 720 b receiving retrograde blood flow whileminimizing the amount of material and bulk added to valve 700. In oneexample of this, similar to the embodiment described in connection withFIG. 4B, second sealing member 720 b may extend partially around thecircumference of stent 702 proximal to the CAFs 716, with first sealingmember 720 a extending partially around the circumference of stent 702proximal to CAFs 716 and proximal to second sealing member 720 b. Inthis embodiment, first sealing member 720 a and second sealing member720 b may each comprise a plurality of individual patches, such asrectangular patches, positioned to catch retrograde blood flow on theabluminal side of stent 702 near the CAFs, which area may beparticularly susceptible to PV leak, as described above in connectionwith FIG. 4B. It should be understood if some other portion of valve 700is determined to be particularly susceptible to PV leak, the sealingmembers 720 a and/or 720 b may be positioned at those locations toincrease the likelihood of mitigating such PV leak.

According to one aspect of the disclosure, a prosthetic heart valvecomprises:

a collapsible and expandable stent body including a generally tubularannulus section;

one or more prosthetic valve elements mounted to the stent body andoperative to allow flow in an antegrade direction but to substantiallyblock flow in a retrograde direction through the annulus section;

a cuff attached to the stent body;

a first sealing member attached to the cuff, the first sealing memberextending circumferentially around an abluminal surface of the stentbody and having an open side facing in a first axial direction and aclosed side facing in a second axial direction opposite to the firstaxial direction so that a flow of blood in the second axial directionwill tend to force blood into the first sealing member and cause thefirst sealing member to billow outwardly relative to the stent body; and

a second sealing member attached to the cuff, the second sealing memberextending circumferentially around the abluminal surface of the stentbody and having an open side facing in the first axial direction and aclosed side facing in the second axial direction so that the flow ofblood in the second axial direction will tend to force blood into thesecond sealing member and cause the second sealing member to billowoutwardly relative to the stent body; and/or

the first sealing member defines a first pocket having a plurality offirst regions, each of the first regions being in fluid communicationwith adjacent ones of the first regions; and/or

the second sealing member defines a second pocket having a plurality ofsecond regions, each of the second regions being in fluid communicationwith adjacent ones of the second regions; and/or

the first sealing member is wrapped around an entire circumference ofthe stent body; and/or

the second sealing member is wrapped around the entire circumference ofthe stent body; and/or

the open side of the first sealing member is attached to the cuff atspaced locations around a circumference of the stent body; and/or

the open side of the second sealing member is attached to the cuff atspaced locations around the circumference of the stent body; and/or

the open side of the first sealing member includes a first plurality ofopenings and the open side of the second sealing members includes asecond plurality of openings, the first plurality of openings beingoffset in a circumferential direction from the second plurality ofopenings; and/or

the first sealing member is positioned nearer an inflow end of the stentbody than the second sealing member; and/or

the open side of the first sealing member is axially spaced apart fromthe closed side of the second sealing member; and/or

the first sealing member comprises an extension of the cuff, theextension being wrapped around an inflow end of the stent body such thatthe extension is positioned on an abluminal surface of the stent body;and/or

a proximal portion of the extension on the abluminal surface of thestent body is connected to a proximal portion of the cuff on the luminalsurface of the stent body with a seam; and/or

the second sealing member is formed from a separate piece of materialfrom the cuff; and/or

the first sealing member is formed from a separate piece of materialfrom the cuff; and/or

the first sealing member is formed of a single piece of material; and/or

the second sealing member is formed of a single piece of material;and/or

the first sealing member is formed from a plurality of pieces ofmaterial; and/or

the second sealing member is formed from a plurality of pieces ofmaterial; and/or

the first sealing member is substantially rectangular; and/or

the second sealing member is substantially rectangular.

Although the prosthetic valves herein have been described with referenceto particular embodiments, it is to be understood that these embodimentsare merely illustrative of the principles and applications of thepresent invention. It is therefore to be understood that numerousmodifications may be made to the illustrative embodiments and that otherarrangements may be devised without departing from the spirit and scopeof the present invention as defined by the appended claims.

It will be appreciated that the various dependent claims and thefeatures set forth therein can be combined in different ways thanpresented in the initial claims. It will also be appreciated that thefeatures described in connection with individual embodiments may beshared with others of the described embodiments.

The invention claimed is:
 1. A prosthetic heart valve, comprising: acollapsible and expandable stent body including a generally tubularannulus section; one or more prosthetic valve elements mounted to thestent body and operative to allow flow in an antegrade direction but tosubstantially block flow in a retrograde direction through the annulussection; a cuff attached to the stent body; a first sealing memberattached to the cuff, the first sealing member extendingcircumferentially around an abluminal surface of the stent body andhaving an open side facing in a first axial direction and a closed sidefacing in a second axial direction opposite to the first axial directionso that a flow of blood in the second axial direction will tend to forceblood into the first sealing member and cause the first sealing memberto billow outwardly relative to the stent body; and a second sealingmember attached to the cuff, the second sealing member extendingcircumferentially around the abluminal surface of the stent body andhaving an open side facing in the first axial direction and a closedside facing in the second axial direction so that the flow of blood inthe second axial direction will tend to force blood into the secondsealing member and cause the second sealing member to billow outwardlyrelative to the stent body, wherein the open sides of the first sealingmember and the second sealing member are attached to the cuff at spacedlocations around a circumference of the stent body so that the open sideof the first sealing member includes a first plurality of openingsoffset in a circumferential direction from a second plurality ofopenings in the open side of the second sealing member.
 2. Theprosthetic heart valve of claim 1, wherein the first sealing memberdefines a first pocket having a plurality of first regions, each of thefirst regions being in fluid communication with adjacent ones of thefirst regions.
 3. The prosthetic heart valve of claim 2, wherein thesecond sealing member defines a second pocket having a plurality ofsecond regions, each of the second regions being in fluid communicationwith adjacent ones of the second regions.
 4. The prosthetic heart valveof claim 1, wherein the first sealing member is wrapped around an entirecircumference of the stent body.
 5. The prosthetic heart valve of claim4, wherein the second sealing member is wrapped around the entirecircumference of the stent body.
 6. The prosthetic heart valve of claim1, wherein the first sealing member is positioned nearer an inflow endof the stent body than the second sealing member.
 7. The prostheticheart valve of claim 6, wherein the open side of the first sealingmember is axially spaced apart from the closed side of the secondsealing member.
 8. The prosthetic heart valve of claim 1, wherein thefirst sealing member comprises an extension of the cuff, the extensionbeing wrapped around an inflow end of the stent body such that theextension is positioned on an abluminal surface of the stent body. 9.The prosthetic heart valve of claim 8, wherein a proximal portion of theextension on the abluminal surface of the stent body is connected to aproximal portion of the cuff on the luminal surface of the stent bodywith a seam.
 10. The prosthetic heart valve of claim 1, wherein thesecond sealing member is formed from a separate piece of material fromthe cuff.
 11. The prosthetic heart valve of claim 10, wherein the firstsealing member is formed from a separate piece of material from thecuff.
 12. The prosthetic heart valve of claim 1, wherein the firstsealing member is formed of a single piece of material.
 13. Theprosthetic heart valve of claim 1, wherein the second sealing member isformed of a single piece of material.
 14. The prosthetic heart valve ofclaim 1, wherein the first sealing member is formed from a plurality ofpieces of material.
 15. The prosthetic heart valve of claim 1, whereinthe second sealing member is formed from a plurality of pieces ofmaterial.
 16. The prosthetic heart valve of claim 1, wherein the firstsealing member is substantially rectangular.
 17. The prosthetic heartvalve of claim 16, wherein the second sealing member is substantiallyrectangular.